Portable Medical Grade Air Purification System

ABSTRACT

A system, method, and air purification device. Air is taken in from an environment into the air purification system. The air is prefiltered. The air is filtered with a primary filter. The filtered air is treated with vacuum ultraviolet radiation in a primary reaction chamber to generate irradiated air. The irradiated air is treated with ultraviolet-C radiation in a secondary reaction chamber to remove ozone. Ozone and other contaminants are removed from the irradiated air utilizing a carbon filter to generate purified air. The purified air is emitted back into the environment from the air purification system.

PRIORITY STATEMENT

This application claims priority to U.S. Provisional Patent ApplicationNo. 63/023,010 filed on May 11, 2020 all of which is hereby incorporatedby reference in their entirety.

BACKGROUND I. Field of the Disclosure

The illustrative embodiments relate to air filtration. Morespecifically, but not exclusively, the illustrative embodiments relateto a system, method, and apparatus for extensive filtering of airparticles in a medical, dental, or other environment.

II. Description of the Art

Recent events have emphasized the important of protecting dentists,doctors, nurses, hygienists, patients, and other individuals fromairborne microorganisms, viruses, pathogens, contaminants, and otherdangerous aerosolized fluids and particulates. It is particularlyimportant to protect healthy individuals from the flu (e.g., H1N1, H5N1,swine influenza, bird influenza, and emerging strains, etc.), COVID-19,biological weapons (e.g., anthrax, small pox, etc.), and other dangerousagents whether natural or man-made. The emergence of COVID-19 has shownthe risks, conditions, and liabilities that medical professionals,businesses, organizations, and individuals are subject to. Many devicesthat have attempted to address air filtering, purification, and/orsterilization have been unable to effectively address the smallestparticles in a format that is user friendly. For example, many arebulky, awkward, or hard to position while others do not effectivelyfilter or sterilize many of the smallest and most dangerousmicroorganisms and particulates in a single pass. Other filtrationdevices are too large or cost prohibitive to be physically andfinancially accessible to most individuals, businesses, medical anddental practices, or other groups.

SUMMARY OF THE DISCLOSURE

The illustrative embodiments provide a medical grade air purificationsystem, method, and device. One embodiment provides a system, method,and air purification device. Air is taken in from an environment intothe air purification system. The air is prefiltered with a prefilter.The air is filtered with a primary filter to generate filtered air. Thefiltered air is treated with vacuum ultraviolet radiation in a primaryreaction chamber to generate irradiated air. The irradiated air istreated with ultraviolet-C radiation in a secondary reaction chamber toremove ozone and contaminants. The ozone and the contaminants areremoved from the irradiated air emitted from the secondary reactionchamber utilizing a carbon filter to generate purified ar. The purifiedair is emitted back into the environment from the air purificationsystem.

The illustrative embodiments provide an air purification system. The airpurification system includes a frame housing various components, theframe is mounted to a plurality of casters for moving the airpurification system between locations. The air purification systemfurther includes a hose extending from an inlet of the frame, the hoseis fixably positioned in three-dimensional space for suctioning air froman environment. The air purification system further includes a prefilterattached to the inlet for receiving the air from the environment. Theair purification system further includes a primary filter proximate theprefilter that further filters the air. The air purification systemfurther includes a primary reaction chamber housing a vacuum ultravioletlight that treats the air and associated contaminants. The primaryreaction chamber is cylindrically shaped to maintain the air proximatethe VUV light to generate irradiated air. The air purification systemfurther includes a secondary reaction chamber interface with the primaryreaction chamber, the secondary reaction chamber housing one or moreultraviolet-C lights for treating the irradiated air to remove ozonegenerated by the primary reaction chamber and to denature thecontaminants. The air purification system further includes a fan thatinterfaces with the secondary reaction chamber to move the air throughthe air purification system. The air purification system furtherincludes a carbon filter that interfaces with the fan to remove ozoneand contaminants from the irradiated air.

In alternative embodiments, the hose includes a nozzle with two or morebutterfly handles for positioning the hose. The nozzle may be coveredwith a moisture control barrier fitted to the nozzle that prefiltersparticulates and aerosols. The air purification system may exclude thehose to treat air in a residential or commercial environment. The airpurification system may be attached to any number of other intakedevices (e.g., hoses, mats, clothing, etc.). The air purification systemmay include a reaction chamber that houses the primary reaction chamberand the secondary reaction chamber. The primary reaction chamber may benested in between portions of the secondary reaction chamber. Theprimary reaction chamber and secondary reaction chamber may be nestedtogether or proximate each other. The nozzle may be covered with adisposable or washable moisture control barrier that prefiltersparticulates and aerosols. The primary filter may represent a HEPA orULPA filter. The air purification system may be mounted on wheels orcasters for easy movement. All or portions of the various components maybe added or removed to different models of the air purification system.The primary reaction chamber may include multiple openings fordispersing the irradiated air into the secondary reaction chamber. Thesecondary reaction chamber may include two or more ultraviolet-C lights.A length and width of the primary reaction chamber may be associatedwith a time period for the air to be treated by VUV radiation from oneor more VUV lights including the VUV light at approximately 180 nm. Thetime period may be at least 0.026 seconds. The air purification systemmay include a hinged top for easily replacing the prefilter, the primaryfilter, ultraviolet bulbs associated with VUV radiation and UVCradiation, and the carbon filter. The air purification system includesone or more catalysts for removing ozone from the irradiated air. Theair purification system may include a power switch for turning the airpurification system on and off. The air purification system may includea controller for controlling the flow rate of air through the airpurification system in cubic feet per minute (or cubic meters perminute). The air purification system may include an interface forviewing and adjusting performance information of the air purificationsystem, maintenance and cleaning reminders, and other relevantinformation. The air purification system may provide alerts regardingperformance, maintenance, and repairs. The alerts may be sent directlyor through one or more networks using a transceiver of the airpurification system. The air purification system may include logic fortracking performance, maintenance, cleaning, and repairs of the airpurification system. The air purification system may include one or moresensors for measuring contaminants in the purified air (e.g., viruses,ozone, etc.).

BRIEF DESCRIPTION OF THE DRAWINGS

Illustrated embodiments are described in detail below with reference tothe attached drawing figures, which are incorporated by referenceherein, and where:

FIG. 1 is a pictorial representation of a medical environment inaccordance with an illustrative embodiment;

FIG. 2 is a pictorial representation of a system including an airpurification system in accordance with an illustrative embodiment;

FIGS. 3-12 are pictorial representations of an air purification systemin accordance with an illustrative embodiment;

FIG. 13 is a flowchart of a process for configuring an air purificationsystem in accordance with an illustrative embodiment;

FIG. 14 is a flowchart of a process for purifying air utilizing an airpurification system in accordance with an illustrative embodiment;

FIG. 15 depicts a computing system in accordance with an illustrativeembodiment;

FIG. 16 is a pictorial representation of the nozzle and intake hose ofFIGS. 3-12 in accordance with illustrative embodiments;

FIG. 17A-D are pictorial representation of portions of the airpurification system of FIGS. 3-12 in accordance with illustrativeembodiments;

FIGS. 18 and 20 are front views of the air purification system of FIGS.3-12 in accordance with an illustrative embodiment;

FIGS. 19A-C are perspective views of portions of the front of the airpurification system in accordance with an illustrative embodiment;

FIG. 21 is a perspective view of the air purification system of FIGS.3-12 in accordance with an illustrative embodiment; and

FIG. 22 is a pictorial representation of a bulb in accordance with anillustrative embodiment.

DETAILED DESCRIPTION OF THE DISCLOSURE

The illustrative embodiments provide a single-pass air purificationsystem that eliminates and eradicates airborne pathogens, contaminants,and microorganisms including bacteria and viruses. The illustrativeembodiments utilize hospital grade HEPA or ULPA air filtration ofbacteria and a vacuum ultraviolet (VUV) reaction chamber which denaturesviruses in a single pass. The VUV reaction chamber utilizes high energyphotons and ozone. The ozone is then subsequently catalyzed to generateclean oxygen using dual-pass UV-C technology and activated carbon. TheUV-C light sources also continue to kill the pathogens. The carbonfilter further eliminates volatile organic compounds, mold spores, andnoxious odors. The illustrative embodiments may be referred to as an airfiltering system, air filtering device, air purification system, airpurification device, air treatment device, advanced filtering andultraviolet irradiation system, air filtration and air purificationsystem, or other similar terminology.

Unlike other filtering devices that rely on multiple passes to killbacteria and denature viruses, the illustrative embodiments produceclean, safe air in the VUV chamber within approximately 0.026 seconds.For example, this means that a 1000 cubic foot room (10′×10′×10′) mayachieve clean air in four minutes on a high setting of 250 cubic feet ofair flow per minute. This filtration is approximately ten times fasterthan existing portable filtering systems to significantly decrease thetransmissibility of airborne pathogens in the healthcare environment.The length of the VUV chamber is associated with an airvelocity/movement providing the sufficient amount of VUV exposure (i.e.,0.026s). The VUV light is effective at inactivation of viruses in ashort time period (e.g., VUV photolysis, irradiation time, generatingreactive oxidants, etc.) due to the high photon energy at 185 nm VUVlight breaking down chemical bonds and disassociating the chemical bondsof the already filtered air. The application of UVC light further treatsthe air for contaminants and reactive oxidants.

The illustrative embodiments further provide a system, method, device,and apparatus for filtering air. The device may perform air filtering,purification, and sterilization using a number of pre-filters, multiplefilters (e.g., ultra-low particulate air (ULPA) filters, high-efficiencyparticulate air (HEPA) filters, etc.) and ultraviolet (UV) lights tokill, neutralize, or sterilize air in any environment. The illustrativeembodiments are configured to perform medical grade filtering andpurification in a single pass rather than relying on multiple passesthrough the system to filter and deactivate applicable contaminants,such as viruses, bacteria, and other microorganisms.

The hose of the device may be positioned and is self-supporting. Thehose may utilize any number of internally or externally supportingstructures to be positioned proximate a patient, medical professional,treatment area, or so forth. As a result, the hose may be moved into afree-standing position extending from the air purification system near apatient, medical professional, or other user in the environment.

The air purification system may include any number of controls forturning the device on and off, setting the flow (e.g., low, medium,high, etc.), adjusting the light sources' intensity,activating/deactivating light sources, performing diagnostics (e.g.,particulates, flow, ozone, power consumption, flow drops, electricalfluctuations, etc.), testing incoming/outgoing air/gases, calibratingthe filtering system, and so forth. The air purification system mayinclude a touch screen, switches, buttons, remote control, or a wirelessinterface (e.g., mobile application communicating through one or moretransceivers to transceivers of the air purification system) forcontrolling the different components, features, and functions of the airpurification system.

The air purification system may also include safety equipment,components, and features, such as fuse breakers, surge protectors,auto-shut off ballasts, fireproof materials, locking wheels/casters,anti-microbial surfaces, quick accessibility for repairs (e.g., hingedlid/top, access panel(s), etc.), maintenance, and replacements, or soforth to ensure the safety of the users and individuals proximate theair purification system.

The illustrative embodiments have particular applicability to addressingissues associated with viral and other outbreaks, such as the 2019 novelcoronavirus referred to commonly as COVID-19, 2019-nCoV, or SARS-CoV-2.The illustrative embodiments provide for enhanced safety and treatmentof various patients in dental offices, surgery centers, hospitals,waiting rooms, or other areas. The embodiments may also be utilized toprotect individuals, families, and groups in any number of residential,commercial or other settings. The illustrative embodiments are mobileand highly effective in filtering and neutralizing various viruses,pathogens, and contaminants. The air purification system may be easilyserviced to change or clean covers, hoses, prefilters, primary filters,fans, or carbon filters. Hinged openings and ports make the variouscomponents highly accessible. Seals and gaskets between the componentskeep everything sealed in an airtight fashion to prevent contaminationbetween the various stages of treated air within the air purificationsystem (e.g., disposable cover, prefiltered air. HEPA/ULPA filtered air,air treated with VUV ultraviolet radiation, air treated with UVCultraviolet radiation, carbon filtered air, etc.). The shapes of thereaction chamber may vary slightly for enhanced manufacturing andimplementation.

The various embodiments, description, functions, and Figures may becombined in any number of combinations and such combinations areexpected regardless of limitations, restrictions, or divisionals createdartificially or naturally.

FIG. 1 is a pictorial representation of a medical environment 100 inaccordance with an illustrative embodiment. The medical environment 100may represent any number of offices, rooms, clinics, spaces, orlocations where medical procedures, surgeries, dental work,examinations, or other processes are performed. The medical environment100 may be within a hospital, clinic, facility, building, mobile unit,or other structure. As with all medical environments, the goal, object,and design of the medical environment 100 is to keep a patient 102, amedical professional 104, and others safe and secure. The medicalenvironment 100 may alternatively represent any number of commercial,residential, or other environments that may benefit from airpurification and filtering.

The patient 102 may represent any number of individuals (human oranimals) that are receiving treatment, assistance, help, or procedures.In some instances, multiple patients may be within the medicalenvironment 100 at a time. The medical professional 104 may representany number of doctors, dentists, surgeons, nurses, technicians,specialists, and other individuals whether professional ornon-professional that may be providing treatment, operating, observing,or otherwise assisting the patient 102.

The air purification system 300 is configured, designed, and provided tofilter, purify, and sterilize the air 101 within the medical environment100. The air 101 includes all of the naturally occurring gases thathumans typically inhale and exhale, whether indoors or outdoors, such asnitrogen, oxygen, argon, carbon dioxide, and other gases. The air 101may also include manmade or introduced gases. The air 101 within themedical environment 100 also includes microorganisms, particulates,fluids, and aerosols that may come from the mouth, nose, orifices, skin,hair, or body of the patient 102 and the medical professional 104,animals/insects, plants/trees, living organisms, dust, objects,equipment, structures, or so forth. The air purification system 300filters the air within the medical environment 100 to remove thepotentially harmful microorganisms (e.g., viruses, bacteria, fungi,etc.), particulates, aerosols, or other contaminants that may bedangerous, unhealthy, harmful, or undesirable to the patient 102 and themedical professional 104.

The air purification system 300 is portable and may be moved fromlocation to location within the medical environment 100. For example,the air purification system 300 may be moved between rooms associatedwith chairs of a dentist office as a dentist, hygienist, orthodontist,endodontist, or other dental professional (i.e., medical professional104) is treating or assisting the patient 102. The air purificationsystem 300 may include casters, wheels, sliders, rails, tracks, or othermechanisms that facilitate the movement of the air purification system300 from location to location.

As is subsequently described, the air purification system 300 mayinclude a hose and nozzle for positioning an intake of the air 101 asclose as possible to the patient 102 and/or medical professional 104. Asa result, the contaminants are extracted from the air 101 as close tothe source (i.e., respiration, operation/procedure site, etc.) so thatthe contaminants do not spread throughout the entire medical environment100. For example, the breath of a potential sick, infected, or otherwisecontaminated patient 102 may be filtered almost immediately upon beingexhaled. The same is equally true for the medical professional 104 andother individuals within the medical environment 100 regardless ofwhether they are sick, infected, or otherwise contaminated whetherknowingly or unknowingly. The nozzle is hygienic and easily cleaned.

The air purification system 300 is configured to be easily moved andpositioned. In one embodiment, the air purification system 300 ispowered through a connection to a standard wall for convenience, such asa standard wall outlet (e.g. 120 V). However, the air purificationsystem 300 may be configured to be powered by any number of powerstandards, wiring/interfaces, systems, or equipment available throughoutthe world. The air purification system 300 may also be battery-poweredfor environments where traditional power systems, connections, wiring,or networks are unavailable or inconvenient.

The air purification system 300 may utilize multiple intake modes tofilter the medical environment 100. As previously described, the hoseand nozzle may act as a directed intake for processing air within themedical environment that is proximate the patient 102 and/or the medicalprofessional 104. The hose and nozzle provide a targeted or patient modethat may be utilized for the air purification system 300. The airpurification system 300 may also be switched into an ambient or fullenvironment mode. In this mode, vents of the air purification system 300are utilized to intake air within the medical environment 100. Thefiltering process utilized by the air purification system 300 in theambient mode is to filter all applicable air within the medicalenvironment 100 without targeting a specific location, patient102/medical professional 104, user, or other segment or section of themedical environment 100. As a result, the air purification system 300may be utilized in various locations, manners, and functions to ensurepatient safety, clean air for entire rooms, or otherwise process air101. The modes may also be referred to as room, hygiene, and operativemodes. The four scenarios in a dental office may be total room—halfpowered, total room—full powered, exam mode—half powered, and operativemode—full powered.

The air purification system 300 is configured to filter, purify,sterilize, or otherwise clean the air within the medical environment 100utilizing a single pass. As a result, a standard sized room may befiltered within a matter of minutes because of the high volume of airflow that is filtered by the air purification system 300. Many existingsystems do not sufficiently filter or treat the air within the medicalenvironment 100 to remove the smallest and often the most dangerousmicroorganisms and contaminants. The illustrative embodiments apply theprinciples of established scientific principles regarding filtering andultraviolet treatment of air 101 to ensure that harmful contaminants areremoved from the medical environment utilizing the air purificationsystem 300.

Unlike many existing systems, the air purification system 300 isconfigured to be easily serviceable by the medical professional 104, hisor her staff, repair or maintenance persons, or other individuals withonly rudimentary understanding of basic device maintenance. As a result,the overall cost, time, and effort associated with the air purificationsystem 300 are reduced while maximizing the filtering results.

It is anticipated that the air purification system 300 may be utilizedin various medical and nonmedical environments, such as to purify rooms,waiting rooms, nail salons, massage rooms, homes, business settings,offices, and other locations where highly purified air is necessary ordesired. The illustrative embodiments may help prevent the spread ofinfectious diseases, particularly those that are airborne.

FIG. 2 is a pictorial representation of a system 200 including an airpurification system 300 in accordance with an illustrative embodiment.In one embodiment, the system 200 of FIG. 2 may include any number ofdevices 201, networks, components, software, hardware, and so forth. Inone example, the system 200 may include a wireless device 202, a tablet204 displaying graphical user interface 205, a laptop 206 (altogetherdevices 201), a network 210, a network 212, a cloud system 214, servers216, databases 218, a data platform 220 including at least a logicengine 222, a memory 224, and data 226. The cloud system 214 may furthercommunicate with third-party resources 230. The various devices,systems, platforms, and/or components may work alone or in combination.

Each of the devices, systems, and equipment of the system 200 mayinclude any number of computing and telecommunications components,devices or elements which may include processors, memories, caches,busses, motherboards, chips, traces, wires, pins, circuits, ports,interfaces, cards, converters, adapters, connections, transceivers,displays, antennas, operating systems, kernels, modules, scripts,firmware, sets of instructions, and other similar components andsoftware that are not described herein for purposes of simplicity. Forexample, the software/applications or hardware may implement all orportions of the processes, methods, and embodiments described herein andshown in the Figures.

For example, the air purification system 300 may include electronics 387including at least wiring 391, power systems 392, sensors 393, atransceiver 394, logic 395, a display 396, a power switch 397, a motorcontrol switch 398, and a power cord 399. The wiring may include one ormore power (e.g., AC, DC, etc.) and communications cords (e.g., serial,parallel, proprietary, etc.) for connecting the various components ofthe air purification system 300. The power systems 392 power the variouscomponents of the air purification system 300 including the electronics387 and a fan (see FIGS. 3-12). The power systems 392 may connect to thepower cord 399 for receiving electricity from a building, generator,structure, or other location. In one embodiment, the power cord 399includes a magnetic interface or break away interface to the body of theair purification system 300 so that the power cord 399 may be removedfrom the air purification system 300 without tripping a user, damagingthe air purification system 300, or otherwise causing damage to a useror the air purification system 300 itself. In one embodiment, portionsof the wiring 391, power systems 392, and other electronics 387 may berun through the false bottom 362. The false bottom 362 (see FIG. 5) is asection near the bottom 342 of the frame 322 (or alternatively sides,back, or top) that separates and protects the various electronics 387.

The sensors 393 may be configured to sense the composition of the airbefore, during, and after the different stages of the purificationprocess. In one embodiment, the sensors 393 include sensors thatdetermine the levels of ozone that are being released by the airpurification system to ensure that the air purification system 300complies with local, State, and Federal laws, statutes, and practices aswell as industry standards. The secondary chamber and other areas withinthe air purification system 300 may also include sensors 393. Thesensors 393 may provide information that may be displayed to the userutilizing the display 396 or communicated through the transceiver 394.The transceiver 394 may communicate with any number devices to displaythe information utilizing a graphical user interface, browser, firmware,operating system/kernel, set of instructions, or an application.

The logic 395 is the processor, digital logic, and circuitry thatprocesses information to implement the processes of the air purificationsystem 300. The logic 395 may include a processor. The processor is thecircuitry or logic enabled to control execution of a set ofinstructions. The processor may be one or more microprocessors, digitalsignal processors, application-specific integrated circuits (ASIC),central processing units, or other devices suitable for controlling theair purification system 300 including one or more hardware and softwareelements, executing software, instructions, programs, and applications,converting and processing signals and information, and performing otherrelated tasks. The processor may be a single chip or integrated withother computing or communications elements. The logic 395 may alsoinclude a memory for storing information regarding the utilization(e.g., total hours on, logged hours, hours in each mode, etc.), aircomposition, environmental conditions (e.g., indoors, outdoors, etc.),networked devices, and so forth. The memory is a hardware element,device, or recording media configured to store data for subsequentretrieval or access at a later time. The memory may be a static ordynamic memory. The memory may include a hard disk, random accessmemory, cache, removable media drive, mass storage, or configurationsuitable as storage for data, instructions, and information. In oneembodiment, the memory and processor may be integrated. The memory mayuse any type of volatile or non-volatile storage techniques and mediums.

The transceiver 394 is a component comprising both a transmitter andreceiver which may be combined and share common circuitry on a singlehousing. The transceiver 394 may communicate utilizing Bluetooth, Wi-Fi,cellular (i.e., 3G, 4G, 5G, PCS, GMSA, etc.), ZigBee, near fieldcommunications, wireless USB, Internet of things (IoT), infrared, mobilebody area networks, ultra-wideband communications, or other radiofrequency standards, networks, protocols, or communications. Forexample, the transceiver 394 may communicate directly with the wirelessdevice 202 or through the network 210. The transceiver 394 may also sendand receive the data 226 through the data platform 220.

The display 396 may communicate relevant information to the userregarding the operation and performance of the air purification system300. The display 396 may communicate information processed by thesensors 393 and/or logic 396. For example, the display 396 maycommunicate total hours, hours per filter, ozone levels, air quality,air composition, ozone levels over time, maintenance and repairreminders (e.g., filter replacement, bulb replacement, etc.), and otherapplicable information. In one embodiment, the display 396 is a lightemitting diode display. In another embodiment, the display 396 may alsoinclude one or more speakers, touch screens, or other interfacecomponents. For example, the display 396 may also be configured toreceive input from the user for setting the mode of operation (i.e.,targeted, ambient, etc.) and settings (e.g., high, low, air flow incubic feet per minute (CFM), etc.).

The power switch 397 may be utilized to turn the air purification systemoff and on. The power systems 392 may include fuses and surge protectorsfor ensuring the safe operation of the air purification system 300.Unexpected power surges may be detected by the power systems 392 to turnoff or otherwise protect the air purification system 300. The motorcontrol switch 398 may be utilized to change the output of the airpurification system (e.g., low, medium, high, etc.) or a custom outputlevel. The power systems 392 may also include an induction power deviceor docking interface, such that when the body of the air purificationsystem 300 is positioned on or above a generation unit, the airpurification system is fully powered. A location may have multiple powergeneration pads or docking pads for powering the air purification system300 when the air purification system 300 is moved to that location.

The system 200 may include any number of air purification systems, suchas the air purification system 300. For example, multiple medicalfacilities and residential locations may all use the system 200. Thesystem 200 may be utilized to process data 226 from numerous airpurification systems 300. The data 226 may include information regardingparticulates, allergens, ozone processing, chemical composition ofprocessed air, weather, and so forth. The data 226 may be utilized totune the performance of the air purification system 300 based onconditions such as humidity, air particulates (e.g., smoke, allergens,dust, etc.), known diseases/pathogens/viruses that are in season, andother applicable information.

In one embodiment, the system 200 may utilize any number of secureidentifiers (e.g., passwords, pin numbers, certificates, etc.), securechannels, connections, links, virtual private networks, biometrics, orso forth to upload, manage, and secure the data 226. Variousauthentications and verifications may be performed to ensure that data226 is true and accurate. The devices 201 utilize any number ofapplications, browsers, gateways, bridges, or interfaces to communicatewith the cloud system 214, platform 220, and/or associated components.The devices 201 may include any number of Internet of Things (IoT)devices, home, and commercial devices.

The data 226 may include a number of different data types. The data 226may include information and data for a number of different airpurifications systems. The data 226 may specify information regardingoperation, performance, ambient conditions, and so forth. For example,the data 226 stored by both the air purification system 300 and in thedata platform 220 may specify total hours of operation, hours for eachfilter/bulb, ambient conditions (e.g., temperature, humidity, etc.),ozone levels (e.g., primary reaction chamber, secondary reactionchamber, expelled air, etc.), processed cubic feet of air (per minute,hour, day, week, year, all time, etc.), and other applicableinformation.

The wireless device 202, tablet 204, and laptop 206 are examples ofcommon devices 201 that may be utilized to capture, receive, and managedata 226 as well as configure and operate the air purification system300. For example, the various devices may capture data relevant to theair purification system 300 that is subsequently utilized or sent to theair purification system 300. Other examples of devices 201 may includee-readers, cameras, video cameras, electronic tags, audio systems,gaming devices, vehicle systems, kiosks, point of sale systems,televisions, smart displays, monitors, entertainment devices, medicaldevices, virtual reality/augmented reality systems, or so forth. Thedevices 201 may communicate wirelessly or through any number offixed/hardwired connections, networks, signals, protocols, formats, orso forth. In one embodiment, the wireless device 202 is a cell phonethat communicates with the network 210 through a 5G connection. Thelaptop 206 may communicate with the network 212 through an Ethernet,Wi-Fi connection, cellular, or other wired or wireless connection. Thedata 226 may be captured based on the permissions, authorization, andconfirmation of the user associated with the air purification system300. The data 226 may also include location-based information andweather information. The data 226 may be utilized to tune performancefor each of a number of air purification systems.

The cloud system 214 may aggregate, manage, analyze, and process data226 and across the Internet, networks 210, 212, other networks, andthird-party resources 230. For example, the networks 210, 212 mayrepresent any number of public, private, virtual, specialty (e.g.,weather, allergy, etc.) or other network types or configurations. Thedifferent components of the system 200, including the devices 201 may beconfigured to communicate using wireless communications, such asBluetooth, Wi-Fi, cellular communications, or so forth. Alternatively,the devices 201 may communicate utilizing satellite connections, Wi-Fi,3G, 4G, 5G, LTE, personal communications systems, DMA wireless networks,and/or hardwired connections, such as fiber optics, T1, cable, DSL, highspeed trunks, powerline communications, and telephone lines. Any numberof communications architectures including client-server, network rings,peer-to-peer, n-tier, application server, mesh networks, fog networks,or other distributed or network system architectures may be utilized.The networks, 210, 212 of the system 200 may represent a singlecommunication service provider or multiple communications servicesproviders.

In one embodiment, the third-party sources 230 may monitor air qualityin one or more medical, commercial, or residential environmentsutilizing the air purification system 300 to ensure compliance withapplicable laws, regulations, standards, and best practices. In oneembodiment, the cloud system 214 (or alternatively the cloud network)including the data platform 220 is specially configured to perform theillustrative embodiments and may be referred to as a system or platform.

The cloud system 214 or network represents a cloud computing environmentand network utilized to aggregate, process, manage, search, verify,generate, and distribute data 226 and communicate with and control theair purification system 300 (based on applicable permissions andauthorizations). The cloud system 214 allows data 226 and specifiedactions (e.g., warnings, communications, updates, configurations, etc.)from multiple businesses, users, managers, or service providers to becentralized. In addition, the cloud system 214 may remotely manageconfiguration, software, and computation resources for the devices ofthe system 200, such as devices 201.

The cloud system 214 may prevent unauthorized access to data 226, tools,and resources stored in the servers 216, databases 218, and any numberof associated secured connections, virtual resources, modules,applications, components, devices, or so forth. In addition, a user maymore quickly upload, aggregate, process, manage, view, and distributedata 226 (e.g., profiles, updates, surveys, content, etc.) whereauthorized, utilizing the cloud resources of the cloud system 214 anddata platform 220.

The cloud system 214 allows the overall system 200 to be scalable forquickly adding and removing air purification systems, users, businesses,authorized sellers, analysis modules, distributors, valuation logic,algorithms, moderators, programs, scripts, filters, distributionpartners, or other users, devices, processes, or resources.Communications with the cloud system 214 may utilize encryption, securedtokens, secure tunnels, handshakes, secure identifiers (e.g., passwords,pins, keys, scripts, biometrics, etc.), firewalls, digital ledgers,specialized software modules, or other data security systems andmethodologies as are known in the art.

The servers 216 and databases 218 may represent a portion of the dataplatform 220. In one embodiment, the servers 216 may include a webserver 217 utilized to provide a website, mobile applications, and userinterface (e.g., user interface 205) for interfacing with numeroususers. Information received by the web server 217 may be managed by thedata platform 220 managing the servers 216 and associated databases 218.For example, the web server 217 may communicate with the database 218 torespond to read and write requests. For example, the servers 216 mayinclude one or more servers dedicated to implementing and recordingcommunications involving the data 226. For example, the databases 218may store a record for updating information relating to data 226 fromthe air purification system.

The databases 218 may utilize any number of database architectures anddatabase management systems (DBMS) as are known in the art. Thedatabases 218 may store the available content associated with each airpurification system 300 which may specify a date of purchase,product/service information (e.g., VUV bulbs, UVC bulbs, carbon filtersprefilters, moisture control barriers, etc.), application, address,residential or commercial application, payment information, permissions,settings, location, cause preferences, cause restrictions, and so forth.Any number of secure identifiers such as passwords, pins, tones, codes,serial numbers, or so forth may be utilized to ensure that content,personal, or transaction information is not improperly shared oraccessed.

The user interface 205 may be made available through the various devices201 of the system 200. In one embodiment, the user interface 205represents one or more of a graphical user interface, audio interface,tactile interface, or other interface that may be utilized to managedata, transactions, and other information. For example, the user mayenter or update associated data for operating the air purificationsystem 300 utilizing the user interface 205 (e.g., browser orapplication on a mobile device). The user interface 205 may be presentedbased on execution of one or more applications, browsers, kernels,modules, scripts, operating systems, or specialized software that isexecuted by one of the respective devices 201. For example, the userinterface 205 may be programmed so that the air purification system 300automatically turns on/off at specified times to specified operationlevels.

The user interface 205 may display current and historical data as wellas trends and projections for operation and performance of the airpurification system 300. The user interface 205 may be utilized to setthe user preferences, parameters, and configurations of the devices 201as well as upload and manage the data, content, and implementationpreferences sent to the cloud system 214. The devices 201 (e.g.,displays, indicators/LEDs, speakers, vibration/tactile components, etc.)may present, play, display, or otherwise communicate the data 226visually, audibly, tactilely, or any combination thereof.

In one embodiment, the system 200 or the cloud system 214 may alsoinclude the data platform 220 which is one or more devices utilized toenable, initiate, generate, aggregate, analyze, process, query, andmanage data 226, and so forth with one or more communications orcomputing devices. The data platform 220 may include one or more devicesnetworked to manage the cloud network and system 214. For example, thedata platform 220 may include any number of servers, routers, switches,or advanced intelligent network devices. The data platform 220 mayrepresent one or more web servers that perform the processes and methodsherein described.

In one embodiment, the logic engine 222 is the logic that controlsvarious algorithms, programs, hardware, and software that interact toreceive, aggregate, analyze, rank, process, manage, score, communicate,and distribute data 226, content, transactions, alerts, reports,messages, or so forth. The logic engine 222 may utilize any number ofthresholds, parameters, criteria, algorithms, instructions, or feedbackto interact with users and interested parties and to perform otherautomated processes. In one embodiment, the logic engine 222 mayrepresent a processor. The processor is circuitry or logic enabled tocontrol execution of a program, application, operating system, macro,kernel, or other set of instructions. The processor may be one or moremicroprocessors, digital signal processors, application-specificintegrated circuits (ASIC), central processing units, or other devicessuitable for controlling an electronic device including one or morehardware and software elements, executing software, instructions,programs, and applications, converting and processing signals andinformation, and performing other related tasks. The processor may be asingle chip or integrated with other computing or communicationselements.

The memory 224 is a hardware element, device, or recording mediaconfigured to store data for subsequent retrieval or access at a latertime. The memory 224 may be a static or dynamic memory. The memory 224may include a hard disk, random access memory, cache, removable mediadrive, mass storage, or configuration suitable as storage for data 226,instructions, and information. In one embodiment, the memory 224 andlogic engine 222 may be integrated. The memory 224 may use any type ofvolatile or non-volatile storage techniques and mediums.

In one embodiment, the cloud system 214 or the data platform 220 maycoordinate the methods and processes described herein as well assoftware synchronization, communication, and processes. The third-partyresources 230 may represent any number of human or electronic resourcesutilized by or in communication with the cloud system 214 including, butnot limited to, businesses, entities, organizations (e.g., medicalassociations), individuals, government databases, private databases, webservers, research services, and so forth.

The third-party resources 230 may represent any number of electronic orother resources that may be accessed to perform the processes hereindescribed. For example, the third-party resources 230 may representgovernment, private, and charitable servers, databases, websites,programs, services, and so forth for verifying the data 226. Any numberof privacy and data policies may be implemented to ensure thatapplicable local, State, Federal, and International laws, standards,practices, and procedures are met.

In one embodiment, the logic engine 222 may utilize artificialintelligence and machine learning. The artificial intelligence andmachine learning may be utilized to enhance data 226 and tune theperformance of one or more air purification systems 300 based onapplicable information (e.g., weather, disease outbreaks, contaminants,etc.).

In another embodiment, the devices 201 may include any number ofsensors, appliances, and devices that utilize real time measurements anddata collection to update the data 226. For example, a sensor network,wearables (e.g., watches, bands, implantable devices, etc.) and Internetof things (IOT) devices may gather user and ambient data. In oneembodiment, the data platform 220 may extract data from third-partyplatforms by opting in and providing user credentials to variousapplications (e.g., Google, Amazon, eBay, Microsoft, etc.) the dataplatform 220 may extract data from the third party sources 230.

FIGS. 3-12 and 16-22 are pictorial representations of an airpurification system 300 in accordance with an illustrative embodiment.FIGS. 3-10 show a partial cut away and exploded views of the airpurification system 300 to better illustrate the various components,integration, functionality, and structure. As shown, the airpurification system 300 may include a nozzle 302, a moisture controlbarrier 304, handles 306, 308, an intake hose 310, and airflowcontroller 314, air control plates 316, 318, a body 321, a frame 322,casters 332, caster locks 334, a hinge 336, a top 338, gaskets 340,bottom 342, side 344, 346, top handles 348, 350, vents 352, guides 354,356, a prefilter 358, a primary filter 360, a false bottom 362, areaction chamber inlet 364, a reaction chamber 366, a primary reactionchamber 368, a secondary reaction chamber 370, light ballasts 372, 374,376, a vacuum ultraviolet (VUV) bulb 378, UVC bulbs 380, 382, a fan 386,a mounting plate 388, vibration mount 398, a carbon filter 390, wiring391, power regulators 392, sensors 393, a transceiver 394, logic 395, adisplay 396, a power switch 397, a motor control switch 398, and a powercord 399.

The intake hose 310 is configured to receive air from the environment ina targeted or specific location or proximate one or more specifiedusers. For example, when the air purification system 300 is operating ina targeted mode, all suction is channeled through the intake hose 310and the associated nozzle 302. In one embodiment, the intake hose 310 isa self-supporting hose. The intake hose 310 may utilize a ribbon-lockconstruction to allow the hose to be positioned, shaped, and reshaped.The hose may be PVC with wire helix reinforcements for maintaining aposition, orientation, and location. The intake hose 310 may be of anylength desired for the selected user and application. In someembodiments, the intake hose 310 may be approximately 6 feet in length.The intake hose 310 and other portions of the air purification system300 may be coated in any number of anti-bacterial, antifungal, or otherdisease resistant coatings, layers, or materials. In one embodiment, theintake hose 310 may include a string of ultraviolet lights or singleflexible light that further treat the air as it passes through theextended length of the intake hose 310. As a result, the air may befurther treated throughout the length of the intake hose.

The length and diameter of the intake hose 310 may be adjusted based onpressure applied by a user by hand or utilizing one or more tools. Inanother embodiment, the intake hose 310 may include any number ofintegrated or attached alms and motors for moving the intake hose 310and corresponding nozzle 302 without the user touching the intake hose310 or the nozzle 302. A processing system of the air purificationsystem 300 may be utilized to move the intake hose 310 and associatednozzle 302 to the correct location. For example, all or portions of theair purification system 300 may be remotely operated utilizing awireless or powerline connection to the air purification system.

The intake hose 310 further includes the nozzle 302. In one embodiment,the nozzle is configured to be positioned proximate one or more users(e.g., patient, doctor, nurse, person undergoing treatment, etc.). Thenozzle 302 may include multiple handles 306, 308 for easily positioningthe suction and of the hose 310. For example, two or more handles 306,308 may allow a medical professional to easily manipulate the nose andattached intake hose 310. The nozzle 302 may attach to the intake hoseutilizing an interference fit, snap, lock, pin, threads, or otherattachment mechanism. The nozzle 302 and the intake hose 310 may beeasily removed to be washed, autoclaved, or otherwise cleaned andsanitized. The nozzle 302 may define any number and size of openings forsuctioning air within an environment. For example, the nozzle 302 mayhave a cone shaped opening to capture a significant amount of air withinan area and to reduce noise created by suctioning the air into thenozzle 302 and intake hose 310. The size and shape of the nozzle 302 mayvary based on the desired suction speed and tolerance for the associatednoise. The nozzle 302 may be formed of any number of antibacterialplastics or other materials. The nozzle 302 is lightweight so that theintake hose 310 does not have significant leverage or moment aims causedby the nozzle 302.

The nozzle 302 may be fitted with a moisture control barrier 304. Themoisture control barrier 304 may be utilized to prefilter largeparticles, aerosols, or moisture before being taken into the airpurification system 300. The moisture control barrier 304 is configuredto be autoclaved, washed, or replaced daily or as needed. The moisturecontrol barrier 304 provides an inexpensive way to quickly and cheaplyremove some of the largest particulates in the medical environment. Themoisture control barrier 304 may include one or more elastics, buttons,straps, hooks, or other mechanisms for securely connecting to the nozzle302. The moisture control barrier 304 fits the size and shape of thenozzle 302. The moisture control barrier 304 may be formed of ananti-bacterial, antifungal, or other materials, coatings, or components.

The intake hose 310 connects to the frame 322 or body 321 of the airpurification system 300 at the intake port 312. The intake port 312 maybe a fixed inlet for connecting to the intake hose 310. For example, theintake port may fit within or on the outside of the intake hose 310. Inaddition, any number of locking mechanisms, snaps, threads, tabs,releases, or other components may be utilized to secure the intake hose310 to the intake port 312. In addition, the intake port 312 may beconfigured to rotate, pivot, or otherwise move to support the movementand positioning of the intake hose 310. The intake port 312 maysimilarly provide a resisted adjustment mechanism so that the intakeport 312 and attached intake hose 310 do not move unless repositioned bya user.

The frame 322 is the support structure and housing for the airpurification system 300. In one embodiment, the frame 322 may representsheet metal that is molded into a rounded rectangular shape as shown.The frame 322 may be powder coated with any number of materials toimprove the ability to clean and maintain the interior and exterior ofthe frame 322. The powder coating may be of a lighter color to ensurethat it matches the other medical, dental, or operating equipment in thearea and to make the air purification system 300 as aestheticallypleasing as possible. The lighter color of the exterior of the frame 322may also show that the device is clean which is important in these typesof environments. As previously described, the frame 322 is composed of afront 324, back 326, top 338, sides 344, 346, and a bottom 342 (all or aportion of which may be removed or accessed through screws, bolts, slideouts, or so forth). The frame 322 may also include the false bottom 362.The bottom 342 includes a number of casters 332. The casters 332 allowthe air purification system 300 to be easily rolled from one location toanother for more effectively positioning the air purification systemincluding the intake hose 310 and the nozzle 302. The casters 332 mayalternatively represent any number of wheels, rollers, slides, railsystems, pulleys, or so forth for moving, lifting, or otherwisepositioning the air purification system 300. The top 338 may include tophandles 348, 350. The top handles 348, 350 may be utilized to move theair purification system 300 from location to location. For example, auser may grab one or more of the top handles 348, 350 to roll the body321 of the air purification system 300 into position.

The top 338 is attached to the back 326 utilizing a hinge 336. The hingeallows the top 338 to be hingedly opened to access the internalcomponents of the air purification system for cleaning, tuning,maintenance, repairs, and replacement. Other portions of the frame 322may be connected utilizing hinges, guides, slides, bolts, screws,rivets, or so forth. The top 338 further includes a latch 328 forsecuring the top to one or more of the front 324 or sides 344, 346. Thetop handle 348 may be utilized to lift the top 338 of the frame 322 oncethe latch 328 is released to access the internal components of the airpurification system 300. The gaskets 340 may seal the various sectionsand components of the air purification system 300. For example, thegaskets 340 may seal the top 338 to the prefilter 358, primary filter360, reaction chamber 366, and other components. The gaskets 340 mayprovide additional integrity for ensuring efficient sealing of the airpurification system 300 to prevent unwanted air leakage.

The air purification system 300 may also be configured to operate in anambient mode. In one embodiment, the front 324 includes a number ofvents 352. When the air purification system 300 is set to the ambientmode, the vents 352 are configured to allow airflow in and through thefront of the air purification system 300. The vents 352 may be utilizedfor receiving ambient air from the environment. The vents 352 may beformed in any number of shapes including slits, rectangles, ordecorative and functional patterns as are shown in FIGS. 3 and 4.

The airflow controller 314 may be utilized to control the mode ofoperation or air intake mode of the air purification system 300. The airflow controller 314 may connect to one or more intake control plates316, 318 (see FIG. 6) that control the air flow into the airpurification system. For example, when the air flow controller 314 ispositioned to the up position as connected to the intake control plate318 (see FIG. 4), the air in the environment is processed through theintake port 312 and intake hose 310. When the air flow controller 314 asconnected to the intake control plate 318 is positioned to the downposition, the air flow enters the frame through the vents 352. Theintake control plates 316, 318 include openings 317, 319 associated withthe intake port 312 and vents 352. When the intake port 312 andassociated opening 317 are positioned to the up or top position based onmovement of the air flow controller 314, the air purification system 300suctions through the intake hose 310. When the air flow controller 314and the opening 319 are positioned to the down or bottom position theair flow is through the vents 352. The vents 352 may be included on boththe front 324 and back 326 of the frame 322 for taking in unpurified airand then expelling purified air.

The cut-away view of FIG. 5 further illustrates the configuration of theprefilter 358, primary filter 360, reaction chamber inlet 364, reactionchamber 366, fan 386, and the carbon filter 390. In one embodiment, adiffuser may be positioned after the intake control plates 316, 318 tofurther spread the air flow through the prefilter 358 and the primaryfilter 360. The diffuser may ensure that all portions of the prefilter358 and the primary filter 360 experience similar wear and usage. Theair scoop 362 may similarly channel the air to the reaction chamberinlet 364 on the backside of the primary filter 360.

The filters are further shown in FIG. 7. The primary filter 360 mayrepresent one or more high-end filters, such as a HEPA or ULPA filter.The air purification device 300 may be specially configured forapplicable environments. The type of primary filter 360 used may varybased on the needed application. For example, the HEPA filter may beused for situations where airflow is prioritized as HEPA filters havebetter airflow than the incredibly dense ULPA filters. ULPA filters maybe utilized when filtering all particulates (including those less than0.1 micron) is the requirement or goal. ULPA filters may decrease theairflow through the air purification system 300 or may require a morepowerful fan 386 and motor. In one embodiment, the prefilter 358 andprimary filter 360 may be 12×24 inches. The width may be approximately 2inches and 6 inches for the prefilter 358 and primary filter 360,respectively. In other embodiments, smaller filters may be utilized withthe air flow channeled to the active portion of the filters. Any numberof holders, positioners, or frames may also be utilized to secure theprefilter 358 and primary filter 360.

In one embodiment, the prefilter 358 and primary filter 360 may beassociated with guides 354, 356 that properly align prefilter 358 andprimary filter 360 within the frame 322. In one embodiment, the guidesare thin metal protrusions, walls, or separators that extend from thesides 344, 346 of the frame 322. The guides 354, 356 appear as finsextending perpendicular to the sides 344, 346 when looking down on theguides 354, 356 from the top of the frame 322. As the air exits theprimary filter 360 it is channeled by the guides 356, walls, or an airscoop to the reaction chamber inlet 364.

FIG. 8 further illustrates the reaction chamber 366. As shown thereaction chamber 366 includes the primary reaction chamber 368 shown asan extended component with opening 365 at the bottom of the primaryreaction chamber 368 and openings 367 at the top of the primary reactionchamber 368. In one embodiment, the primary reaction chamber 368 may bea partially hexagonal or octagonal shape with another side of theprimary reaction chamber 368 being rectangular, the two sides beingintegrated. In another embodiment, the primary reaction chamber 368 maybe a cylinder or rectangle. The length of the reaction chamber 366 issufficiently long to include the VUV bulb 378 and the UVC bulbs 380,382and associated housing, mounting, and electronic components. The opening365 is affixed to the primary reaction chamber inlet 368. For example,one or more mounting plates, collars, tabs, or other connectors may beutilized to secure the primary reaction chamber 368 to the reactionchamber inlet 364. The primary reaction chamber 368 houses at least oneVUV bulb 378. The vacuum ultraviolet radiation emitted by the VUV bulb378 emits radiation whose spectrum is approximately 185 nm. Many VUVbulbs emit 185 nm ultraviolet radiation that propagate effectively wellthrough nitrogen in air, necessitating the need to keep the air in closeproximity to the VUV bulb 378. The primary reaction chamber 368 performsultraviolet photocatalytic oxidation (PCO). The VUV bulb 378 is idealfor disinfection of air because of the high efficiency for inactivatingbacteria and protozoa. In particular, the VUV bulb 378 damages cellwalls, membranes, enzymes, and nucleic acids of bacteria and damagesvirus proteins and genome of microorganisms in a very short time. TheVUV bulb 378 may also generate ozone, hydroxyl radicals, and reactiveoxygen species (ROS). The primary reaction chamber 368 is sized suchthat at an ideal airflow of 250 cfm, the microorganisms in the air aredenatured while limiting the amount of ozone generated during the PCOprocess. Scientific research has shown that air (e.g., withcontaminants, such as viruses) needs approximately 0.026 seconds bedenatured by a VUV bulb 378. That would require that the primaryreaction chamber 368 be at least twelve inches (12″) long. To provideadditional margins of error, the primary reaction chamber 368 may beapproximately twenty inches long (20″) providing the air within thereaction chamber approximately 0.046 seconds within the primary reactionchamber 368 where the VUV radiation may denature and sterilize the airparticles from multiple angles.

The VUV bulb 378 is centered within the primary reaction chamber 368. Asa result, the particles in the air are quickly denatured before beingexpelled through the openings 367 into the secondary reaction chamber370. The primary reaction chamber 368 may be cylindrically shaped sothat the airflow is evenly centered around the VUV bulb 378. In otherembodiments, the primary reaction chamber 368 may be an extendedrectangle. The openings 367 allow the air to dissipate the pressure inthe primary reaction chamber 368 quickly for treatment in the secondaryreaction chamber 370.

The secondary reaction chamber 370 may be rectangularly shaped withopenings associated with the primary reaction chamber inlet and the fanoutlet. The secondary reaction chamber 370 includes a number of UVCbulbs 380, 382. For example, one, two, four, eight, or more UVC bulbs380, 382 may be mounted within the secondary reaction chamber 370 totreat the air expelled from the primary reaction chamber 368. Inaddition, UVC bulbs 380, 382 emit a wavelength that further degradesozone. The UVC bulbs 380, 382 act as a photocatalyst to break down ozonethat is generated by the VUV bulb 378 in the primary reaction chamber368. Each of the VUV bulb 378 and the UVC bulbs 380, 382 are connectedto light ballasts 372, 374, 376. The secondary reaction chamber 370 mayinclude any number of fins, gates, or guides for guiding the airflowwithin the secondary reaction chamber 370, ensuring that there is timefor the air to be treated by the UVC bulbs 380, 382. In one embodiment,the fins, gates, or guides may include or be coated with a catalyst forfurther neutralizing microorganisms and for degrading ozone. Forexample, the fins, gates, or guides may utilize a corrugated structureand may be composed of Pt, Pd, Ru, Cu, W, Sn, Rh, Ce, Al₂0₃, SiO₂, TiO₂,ZrO₂, metal oxides (e.g., manganese oxide, nickel oxide, iron oxide,etc.), and others. Any number of catalysts may be used within the airpurification system 300 once the air is treated by the VUV bulb 378. Thecatalysts may be corrugated or otherwise structured to maximize surfacearea. Titanium palladium catalysts may be particularly helpful fortreating the ozone and contaminants.

In one embodiment, the reaction chamber 366 may be coated withreflective materials, such as polished aluminum or other materials thatreflect ultraviolet light, such that the air is treated from all sides(e.g., initially emissions, reflections, etc.). The reaction chamber 366may also be described as the primary reaction chamber 368 housed withinthe secondary reaction chamber 370 to make effective use of space andquickly treat the air including all potential particles. The reactionchamber 366 is particularly effective at treating particles that are 0.3microns or smaller including the smallest viruses.

The light ballasts 372, 374, 376 may fit one, all, or multiple bulbs ofthe air purification system 300. The light ballasts 372, 374, 376 may bepowered by one or more power systems 392. The power systems 392 mayinclude one or more amplifiers, regulators, transformers, and otherapplicable equipment for ensuring the safe electrical operation of theair purification system 300. The power systems 392 may provide power tothe light ballasts 372, 374, 376 and the fan 386.

The reaction chamber 366 allows multiple different wavelengths ofultraviolet light to be applied to the air to both neutralizemicroorganisms and remove ozone and other radicals generated based onthe operation of the VUV bulb 378. The reaction chamber 366 alsoefficiently utilizes space maximizing the time during which air istreated by the ultraviolet lights when flowing through the reactionchamber 366 while reducing the space required for airflow.

The air purification system 300 may further include separators 359, 361,363. The separators 359, 361, 363 prevent unwanted airflow through theair purification system. One or more edges or openings defined by theseparators 359, 361, 363 as shown may include seals, gaskets, orseparators to ensure that there is not leakage of air between thevarious components of the air purification system 300 that are unwanted.The separator 359 separates the primary filter 360 from the reactionchamber 366. The reaction chamber 366 including the primary reactionchamber 368 and the secondary reaction chamber 370 may be removed fromthe frame 322 for maintenance and cleaning as needed.

The fan 386 is mounted to the bottom 342, sides 344, 346, or separators361, 363 utilizing a mounting plate 388 and/or vibrations mounts 389which may include a plate and rubber separator. The fan 386 is mountedto reduce the noise produced by the air purification system 300 based onnoise, vibration, movement of air, and so forth. The fan 386 isindustrial strength and provides the suction at the nozzle 302 andintake hose 310 that drives the airflow through the air purificationsystem 300. The fan 386 is also powered by the power systems 392.

The fan 386 draws air from the reaction chamber 366 and expels the airinto the carbon filter 390. The carbon filter 390 further removesmicroorganisms and the ozone generated by the interaction of the airwith the VUV bulb 378. As a result, the ozone levels of the purified airleaving the air purification system 300 are negligible when expelledfrom the air purification system 300.

The carbon filter 390 includes carbon in a dust, microstructure, orcompressed format that filters the air to remove contaminants as well asozone. In one embodiment, the carbon filter 390 is a mesh receptacle forholding carbon (e.g., powder, particulates, etc.) that may be easilyremoved and replaced as needed. The carbon filter 390 may also includeone or more screens, lattices, or additives that act as catalysts forneutralizing microorganisms, removing ozone, and degrading radicalelements and compounds that may be created during the filtrationprocess.

The carbon filter 390 may represent a single structure that has beencompressed, adhered, molded, or otherwise generated or fixed as a singleunit that may be added or removed from the air purification system 300.The carbon filter 390 may also have guides for easily adding andremoving the carbon filter 390 from the air purification system 300.

It is expected that the prefilter 358, primary filter 360, VUV bulb 378,and UVC bulbs 380, 382, and carbon filter 390 will be replaced yearly toensure effective operation.

FIG. 13 is a pictorial representation of a flowchart of a process forpositioning an air purification system in accordance with anillustrative embodiment. The process of FIG. 13 may be performed by anair purification system, such as the air purification system 300 ofFIGS. 3-12. In one embodiment, a user may perform the process of FIG.13. In another embodiment, the air purification system may be equippedto handle audio/verbal, gesture, or other commands from the user toperform the process of FIG. 13. One or more remote controls or devicesexecuting an application or web interface may also be utilized tocontrol the air purification system.

The process may begin by positioning a body of the air purificationsystem (step 1302). The body of the air purification system mayrepresent the main structure and frame of the air purification system.The body is where the majority of the air filtering, purification, andsterilization processes are performed. The body may be mounted oncasters, wheels, or rollers for easily moving the air purificationsystem into place. The air purification system may also have handlesthat may be utilized to lift and/or move the air purification systemfrom one point to another. In one embodiment, the air purificationsystem may include a locking mechanism or stopper for fixing the airpurification system at a single point. For example, locks of one or morecastor wheels may ensure that the air purification system does not moveor roll during utilization. The air purification system mayalternatively use lifts, stops, kickstands, suction cups, magnets, orother devices for being fixed in place. In other embodiments, the airpurification system may not include wheels or casters and may instead besemi-permanently positioned or fixed in place utilizing a plate,brackets, frame, or other mechanisms for securing the air purificationsystem the floor, walls, ceiling, freely suspended, or so forth.

Next, the process continues by ensuring that the air purification systemis safely powered (step 1304). In one embodiment, the air purificationsystem may be powered through a standard 3-prong wall outlet (e.g., 120V US outlet). The air purification system may also be powered by anynumber of standard or proprietary connections available within ahospital, clinic, dental office, mobile treatment unit, or other similarlocation. In alternative embodiments, the air purification system may bebattery powered. The air purification system may also be powered bysolar cells, fuel cells, hand crank, wind turbine, or other similarprocesses, systems, equipment, or so forth. In another embodiment, theair purification system may include a motion detector for automaticallypowering the air purification system on in response to detecting one ormore users in the area. Similarly, the air purification system may turnitself off after not sensing any motion for a time period (e.g., fiveminutes).

Next, the process positions the nozzle and hose to interface with one ormore users (step 1306). The hose is self-supporting and may be movedinto any number of positions, locations, or orientations. The diameterand length of the hose may correspond to the needs of the user of theair purification system. In some instances, a 4-foot hose may besufficient while in others an 8 foot or longer hose may be required. Inone embodiment, the nozzle and hose may be proximate one or more userswithout being so close as to be disruptive, loud, annoying, in the way,or inconvenient. In other embodiments, the air purification system mayinclude multiple hoses and nozzles for targeting numerous areas within aspecific location at one time. For example, the hose may split in twofor two patients that are near each other in the same room. The suctionend of the hose and nozzle may also vary. In one embodiment, the hosemay connect to a bib, collar, blanket, hat, vent, or other device wornor proximate the user.

Next, the process turns on the air purification system to a selectedlevel (step 1308). The air purification system may include one or morelevels for filtering and purifying the air. For example, the airpurification system may have a low setting and a high setting. The airpurification system may also be adjusted between multiple modes. Forexample. during step 1308, the air purification system may be set to atargeted mode that utilizes the hose and nozzle or to an ambient modethat utilizes vents on the front of the air purification system. Somevariations of the air purification system may only be configured forutilizing the hose and nozzle or the integrated vents.

Next, the process repositions the nozzle and hose as needed (step 1310).The hose and nozzle may be moved or repositioned as needed based on theneeds of one or more medical professionals, patients, or other users.For example, the medical professional may need to move from one locationand/or position to another resulting in the need to similarly repositionthe nozzle and hose. In addition, the body of the air purificationsystem may also be rolled, positioned, moved, or maneuvered during step1310.

FIG. 14 is a flowchart of a process for purifying air utilizing an airpurification system. The process of FIG. 14 may be performed by an airpurification system, such as the air purification system 300 of FIGS.3-12. The process may begin by drawing, air into a nozzle of the airpurification system (step 1402). The air purification system may bepowered by one or more fans, motors, or other devices that createsuction and airflow through the air purification system. In analternative embodiment, the airflow may be generated by one or morevacuums, central air systems, portable motors, or so forth. Aspreviously disclosed, the nozzle may have numerous shapes, sizes, orinterfaces for suctioning air from an environment. Targeted nozzles orlarger vented attachments may also be utilized. In one embodiment, thehose of the air purification system may be compatible with nozzlestypically used by vacuum cleaners, standard air filters, or otherapplicable devices.

Next, the air purification system filters air through a moisture controlbarrier (step 1404). The moisture control barrier may represent anynumber of cloth, paper, material, or other attachments that may bepositioned over, on, or integrated with the nozzle and/or hose of theair purification system. The moisture control barrier is configured tobe easily cleaned, autoclaved, or sanitized. Alternatively, the moisturecontrol barrier may be disposed of and a new moisture control barrierutilized each day, for different patients, or so forth. The moisturecontrol barrier may include any number of attachment components such aselastics, straps, buttons, hooks, hook-and-loop fasteners, adhesives,ties, or so forth.

Next, the air purification system filters the air through the prefilter(step 1406). The prefilter is configured to remove large particulatesand organisms to better preserve the capacity of the main or primaryfilter. The prefilter may be more cheaply replaced as needed. Forexample, the main filters may represent HEPA or open filters that aremuch more expensive.

Next, the air purification system filters the air through the primaryair filter (step 1408). The primary air filter may remove particles ofvarying size based on the application. In some embodiments moreaffordable filters may be utilized, as the primary filter because of theeffectiveness of the UV treatments that are implemented by the airpurification system. As a result, the air purification system is muchcheaper than existing systems while still providing equivalent or betterfiltration results.

Next, the air purification system treats the air with vacuum ultravioletlight in a primary reaction chamber (step 1410). In one embodiment, thewavelength of the ultraviolet light may be approximately 185 nm foreffectively degrading and breaking down even the smallest bacteria,viruses, and other bio contaminants. The VUV bulbs utilized may destroythe contaminants utilizing photonic emissions and ozone. The airpurification system may utilize one or more reaction chambers with oneor more VUV bulbs.

Next, the air purification system treats the air with ultraviolet-Clight in the secondary reaction chamber (step 1412). In one embodiment,ultraviolet-C may be in the 200-280 nm wavelength. The secondaryreaction chamber further sterilizes the air and degrades the ozonegenerated by the application of VUV light.

Next, the air purification system filters the air through a carbonfilter (step 1414). The carbon filter further purifies the air andremoves ozone. The carbon filter in step 1414 may represent a solidfilter, carbon dust/particulates, or other composition. The airpurification system may have a venting system for evenly ordirectionally venting the purified air. In another embodiment, scents ordeodorizers may be introduced into the vented air as part of the airpurification system.

Next, the air purification system expels the air from the airpurification system (step 1416). The air purification system may beconfigured to purify between 50-500 cfm. In one embodiment, the airpurification system processes air at approximately 250 cfm. The airquality of the air expelled, emitted, or otherwise communicated throughthe air purification system may be tested for ozone, composition,temperature, and other factors. In one embodiment, the air purificationsystem may turn off completely or shut down the VUV bulb in response todetermining the ozone levels are too high. For example, the airpurification system may employ an automatic shut off in response toozone levels exceeding 20 parts per billion (ppb).

In another embodiment, the intake hose may be connected to the outlet(closed loop) to ensure that the air purification system/device is fullysanitized. In another embodiment, the intake may also be preloaded withozone utilizing an ozone generator or VUV bulb within or near the intakehose. In another embodiment, the air purification system may be coveredwith a plastic or material cover with openings for the vents on thefront and back of the device. The cover may match the aesthetic of thelocation or may make the air purification system appear more desirableto children (e.g., elephant, giraffe, or anteater covers). In anotherembodiment, the air purification system may not include a fan/motor andmay instead be powered as needed by a suction device, such as a commonvacuum or central vacuum system. In another embodiment, the reactionchamber may be large enough to allow personal protective equipment,tools, or other materials to be placed within the air purificationsystem for sterilization.

The illustrative embodiments may take the form of an entirely hardwareembodiment, an entirely software embodiment (including firmware,resident software, micro-code, etc.) or an embodiment combining softwareand hardware aspects that may all generally be referred to herein as a“circuit,” “module” or “system.” Furthermore, embodiments of theinventive subject matter may take the form of a computer program productembodied in any tangible or non-transitory medium of expression havingcomputer usable program code embodied in the medium. The describedembodiments may be provided as a computer program product, or software,that may include a machine-readable medium having stored thereoninstructions, which may be used to program a computing system (or otherelectronic device(s)) to perform a process according to embodiments,whether presently described or not, since every conceivable variation isnot enumerated herein. A machine-readable medium includes any mechanismfor storing or transmitting information in a form (e.g., software,processing application) readable by a machine (e.g., a computer). Themachine-readable medium may include, but is not limited to, magneticstorage medium (e.g., floppy diskette); optical storage medium (e.g.,CD-ROM); magneto-optical storage medium; read only memory (ROM); randomaccess memory (RAM); erasable programmable memory (e.g., EPROM andEEPROM); flash memory; or other types of medium suitable for storingelectronic instructions. In addition, embodiments may be embodied in anelectrical, optical, acoustical or other form of propagated signal(e.g., carrier waves, infrared signals, digital signals, etc.), orwireline, wireless, or other communications mediums.

Computer program code for carrying out operations of the embodiments maybe written in any combination of one or more programming languages,including an object-oriented programming language such as Java,Smalltalk, C++ or the like and conventional procedural programminglanguages, such as the “C” programming language or similar programminglanguages. The program code may execute entirely on a user's computer,partly on the user's computer, as a stand-alone software package, partlyon the user's computer and partly on a remote computer or entirely onthe remote computer or server. In the latter scenario, the remotecomputer may be connected to the user's computer through any type ofnetwork, including a local area network (LAN), a personal area network(PAN), or a wide area network (WAN), or the connection may be made to anexternal computer (e.g., through the Internet using an Internet ServiceProvider).

FIG. 15 depicts a computing system 1500 in accordance with anillustrative embodiment. For example, the computing system 1500 mayrepresent a device, such as one or more of the devices 201 of FIG. 2.The computing system 1500 includes a processor unit 1001 (possiblyincluding multiple processors, multiple cores, multiple nodes, and/orimplementing multi-threading, etc.). The computing system includesmemory 1007. The memory 1007 may be system memory (e.g., one or more ofcache, SRAM, DRAM, zero capacitor RAM, Twin Transistor RAM, eDRAM, EDORAM, DDR RAM, EEPROM, NRAM, RRAM, SONOS, PRAM, etc.) or any one or moreof the above already described possible realizations of machine-readablemedia. The computing system also includes a bus 1003 (e.g., PCI, ISA,PCI-Express, HyperTransport®, InfiniBand®, NuBus, etc.), a networkinterface 1005 (e.g., an ATM interface, an Ethernet interface, a FrameRelay interface, SONET interface, wireless interface, etc.), and astorage device(s) 1009 (e.g., optical storage, magnetic storage, etc.).The system memory 1007 embodies functionality to implement embodimentsdescribed above. The system memory 1007 may include one or morefunctionalities that store user data (including transactions), content,blockchain data, tokens, ledgers, parameters, application, userprofiles, and so forth. Code may be implemented in any of the otherdevices of the computing system 1500. Any one of these functionalitiesmay be partially (or entirely) implemented in hardware and/or on theprocessing unit 1001. For example, the functionality may be implementedwith an application specific integrated circuit, in logic implemented inthe processing unit 1001, in a co-processor on a peripheral device orcard, etc. Further, realizations may include fewer or additionalcomponents not illustrated in FIG. 15 (e.g., video cards, audio cards,additional network interfaces, peripheral devices, etc.). The processorunit 1001, the storage device(s) 1009, and the network interface 1005are coupled to the bus 1003. Although illustrated as being coupled tothe bus 1003, the memory 1007 may be coupled to the processor unit 1001.

FIG. 16 is a pictorial representation of the nozzle 302 and intake hose310 of FIGS. 3-12 in accordance with an illustrative embodiment. Asshown, the nozzle 302 may include handles 306, 308 for easily moving thenozzle 302 and associated intake hose 310 into position. The handles306, 308 may also be referred to as butterfly handles because of theirshape and configuration. In one embodiment, the nozzle 302 is formed orcoated with antibacterial materials. In another embodiment, the nozzle302 may include an external UV light for sterilizing the outer surfaceof the nozzle 302. In another embodiment, the nozzle 302 may include oneor more indicators that indicate the direction of the nozzle. Forexample, lights, lasers, or other projection components may be utilized.

FIG. 22 is a pictorial representation of a VUV bulb 378 in accordancewith an illustrative embodiment. The VUV bulb 378 may represent anynumber of ultraviolet bulbs or lights (e.g., light emitting diode, bulb,lasers, optical resonators, etc.). The VUV bulb 378 may also representthe UVC bulbs or lights herein described.

The features, steps, and components of the illustrative embodiments maybe combined in any number of ways and are not limited specifically tothose described. In particular, the illustrative embodiments contemplatenumerous variations in the smart devices and communications described.The foregoing description has been presented for purposes ofillustration and description. It is not intended to be an exhaustivelist or limit any of the disclosure to the precise forms disclosed. Itis contemplated that other alternatives or exemplary aspects areconsidered included in the disclosure. The description is merelyexamples of embodiments, processes or methods of the invention. It isunderstood that any other modifications, substitutions, and/or additionsmay be made, which are within the intended spirit and scope of thedisclosure. For the foregoing, it can be seen that the disclosureaccomplishes at least all of the intended objectives.

The illustrative embodiments are not to be limited to the particularembodiments and examples described herein. In particular, theillustrative embodiments contemplate numerous variations in the type ofways in which embodiments of the invention may be applied to airfiltering, purification, and sterilization. The foregoing descriptionhas been presented for purposes of illustration and description. It isnot intended to be an exhaustive list or limit any of the disclosure tothe precise forms disclosed. It is contemplated that other alternativesor exemplary aspects are considered included in the disclosure. Thedescription is merely examples of embodiments, processes or methods ofthe invention. It is understood that any other modifications,substitutions, and/or additions may be made, which are within theintended spirit and scope of the disclosure. For the foregoing, it canbe seen that the disclosure accomplishes at least all of the intendedobjectives.

The previous detailed description is of a small number of embodimentsfor implementing the invention and is not intended to be limiting inscope. The following claims set forth a number of the embodimentsdisclosed with greater particularity.

What is claimed is:
 1. A air purification system, comprising: a frame housing various components, the frame is mounted to a plurality of casters for moving the filtering device between locations; a hose extending from an inlet of the frame, the hose is fixably positioned in three-dimensional space for suctioning air from an environment; a prefilter attached to the inlet for receiving the air from the environment; a primary filter proximate the prefilter that further filters the air; a primary reaction chamber housing a vacuum ultraviolet (VUV) light that treats the air and associated contaminants, wherein the primary reaction chamber is cylindrically shaped to maintain the air proximate the VUV light to generate irradiated air; a secondary reaction chamber interfaces with the primary reaction chamber, the secondary reaction chamber housing one or more ultraviolet-C lights for treating the irradiated air to remove ozone generated by the primary reaction chamber and to denature the contaminants; a fan interfaces with the secondary reaction chamber to move the air through the air purification system; and a carbon filter interfaces with the fan to remove ozone and contaminants from the irradiated air.
 2. The air purification system of claim 1, wherein the hose includes a nozzle with two or more butterfly handles for positioning the hose.
 3. The air purification system of claim 1, wherein a moisture control barrier is attached to the nozzle for prefiltering particulates and aerosols.
 4. The air purification system of claim 1, wherein the primary filter represents a high-efficiency particulate air (HEPA) filters or ultra-low particulate air (ULM) filter.
 5. The air purification system of claim 1, wherein the primary reaction chamber is housed, within the secondary reaction chamber.
 6. The air purification system of claim 1, wherein the primary reaction chamber includes multiple openings for dispersing the irradiated air into the secondary reaction chamber, wherein the secondary reaction chamber includes two or more ultraviolet-C lights.
 7. The air purification system of claim 1, wherein a diameter and length of the primary reaction chamber are associated with a time period for the air to be treated by the vacuum ultraviolet radiation at approximately 180 nm.
 8. The air purification system of claim 7, wherein the time period is at least 0.026 seconds.
 9. The air purification system of claim 1, wherein the frame includes a hinged top for easily replacing the prefilter, the primary filter, the VUV light, the ultraviolet-C lights, and the carbon filter.
 10. A method for air purification, comprising: intaking air from an environment into an air purification system; prefiltering the air with a prefilter; filtering the air with a primary filter to generate filtered air; treating the filtered air with vacuum ultraviolet radiation in a primary reaction chamber to generate irradiated air; treating the irradiated air with ultraviolet-C radiation in a secondary reaction chamber; removing ozone and other contaminants from the irradiated air emitted from the secondary reaction chamber utilizing a carbon filter to generate purified air; emitting the purified air back into the environment through the air purification system.
 11. The method of claim 10, further comprising: prefiltering the air from the environment with a moisture control barrier.
 12. The method of claim 11, wherein the moisture control barrier fits on a nozzle of an intake hose.
 13. The method of claim 11, wherein the primary filter is a HEPA or ULPA filter.
 14. The method of claim 11, wherein the air purification system includes a hinged top for easily replacing the prefilter, the primary filter, ultraviolet bulbs associated with the vacuum ultraviolet radiation and the ultraviolet-C radiation, and the carbon filter.
 15. The method of claim 11, further comprising: catalyzing the irradiated air to remove ozone utilizing one or more catalysts.
 16. The method of claim 11, further comprising: shutting down the ultraviolet irradiation and/or air purification system in response to ozone levels emitted from the air purification system exceeding a threshold.
 17. The method of claim 11, wherein the carbon filter includes a catalyst for further removing ozone from the filtered air received from the secondary reaction chamber.
 18. The method of claim 11, wherein a diameter and length of the primary reaction chamber are associated with a time period for the air to be treated by the vacuum ultraviolet radiation at approximately 180 nm.
 19. The method of claim 11, wherein the primary reaction chamber is within a reaction chamber that also includes the secondary reaction chamber.
 20. The method of claim 11, wherein one or more channels divert airflow within the secondary chamber to prolong exposure of the irradiated air to the ultraviolet-C radiation to remove ozone and treat the air for contaminants. 